SE-ATLAS

Cerebral sinovenous thrombosis Calpain-3-related limb-girdle muscular dystrophy R1 Hereditary hyperekplexia Classic stiff person syndrome Focal stiff limb syndrome Limbic encephalitis with LGI1 antibodies Progressive encephalomyelitis with rigidity and myoclonus Multifocal motor neuropathy Acute disseminated encephalomyelitis Huntington disease Autosomal dominant progressive external ophthalmoplegia Facioscapulohumeral dystrophy Mitochondrial DNA-related progressive external ophthalmoplegia Steinert myotonic dystrophy Marfan syndrome Tuberculous meningitis Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Hereditary spastic paraplegia Leukodystrophy Rare dystonia Hereditary neuropathy with liability to pressure palsies Limb-girdle muscular dystrophy Lambert-Eaton myasthenic syndrome Multiple system atrophy, cerebellar type Progressive supranuclear palsy Blepharospasm-oromandibular dystonia syndrome MELAS Lyme disease Meningioma Neuromyelitis optica spectrum disorder Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Muscular dystrophy Progressive muscular atrophy Sporadic Creutzfeldt-Jakob disease Primary angiitis of the central nervous system Myasthenia gravis Limbic encephalitis Guillain-Barré syndrome Fragile X-associated tremor/ataxia syndrome Proximal spinal muscular atrophy type 3 FKRP-related limb-girdle muscular dystrophy R9 Persistent idiopathic facial pain Autosomal dominant cerebellar ataxia Dermatomyositis Becker muscular dystrophy Myofibrillar myopathy Duchenne muscular dystrophy Distal myopathy Susac syndrome Neuralgic amyotrophy Glioblastoma Proximal myotonic myopathy Proximal spinal muscular atrophy type 2 Kennedy disease Corticobasal syndrome Late-onset distal myopathy, Markesbery-Griggs type Autosomal recessive axonal neuropathy with neuromyotonia Inclusion body myositis Dopa-responsive dystonia Isolated dystonia Thomsen and Becker disease Leber hereditary optic neuropathy Autosomal recessive limb-girdle muscular dystrophy Behçet disease Giant cell arteritis Primary lateral sclerosis Stiff person spectrum disorder Moyamoya disease NMDA receptor encephalitis Hypokalemic periodic paralysis Familial Mediterranean fever Meningococcal meningitis Anoctamin-5-related limb-girdle muscular dystrophy R12 Reversible cerebral vasoconstriction syndrome Immune-mediated necrotizing myopathy CLIPPERS Chronic inflammatory demyelinating polyneuropathy Herpes simplex virus encephalitis Autosomal recessive progressive external ophthalmoplegia Limbic encephalitis with caspr2 antibodies Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy Glycogen storage disease due to acid maltase deficiency Multiple system atrophy, parkinsonian type Idiopathic intracranial hypertension Hereditary ATTR amyloidosis Amyotrophic lateral sclerosis Wilson disease Trigeminal neuralgia Glial tumor SUNCT syndrome